JP3188583B2 - Magnesium supplements and their use - Google Patents

Magnesium supplements and their use

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Publication number
JP3188583B2
JP3188583B2 JP05103994A JP5103994A JP3188583B2 JP 3188583 B2 JP3188583 B2 JP 3188583B2 JP 05103994 A JP05103994 A JP 05103994A JP 5103994 A JP5103994 A JP 5103994A JP 3188583 B2 JP3188583 B2 JP 3188583B2
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JP
Japan
Prior art keywords
magnesium
supplement
present
deficiency
diet
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP05103994A
Other languages
Japanese (ja)
Other versions
JPH0769902A (en
Inventor
篤胤 太田
星吾 馬場
嘉夫 森山
登志雄 滝沢
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Meiji Seika Kaisha Ltd
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Meiji Seika Kaisha Ltd
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Publication date
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Priority to JP05103994A priority Critical patent/JP3188583B2/en
Publication of JPH0769902A publication Critical patent/JPH0769902A/en
Application granted granted Critical
Publication of JP3188583B2 publication Critical patent/JP3188583B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、マグネシウム補給材
その利用に関し、詳しくは吸収性に優れ、マグネシウム
欠乏に起因する種々の病的症状の改善効果を有するマグ
ネシウム補給材とその利用に関するものである。
BACKGROUND OF THE INVENTION This invention is, and magnesium supplementation material
More specifically, the present invention relates to a magnesium supplement having excellent absorbability and an effect of improving various pathological symptoms caused by magnesium deficiency, and its use .

【0002】[0002]

【従来の技術および発明が解決しようとする課題】マグ
ネシウムは、生体内で多くの酵素反応に関与しているミ
ネラルである。また、マグネシウムは生体内においては
骨に多く存在しているため、その欠乏は骨粗鬆症,骨軟
化症の原因となる。さらに、マグネシウムは同じ二価の
イオンであるカルシウムの生体内分布にも関与してお
り、その欠乏により腎臓結石などの異所性の石灰化が起
こる。これ以外にもマグネシウムの欠乏は、糖尿病,高
血圧症といった疾患の一因であると考えられている。
BACKGROUND OF THE INVENTION Magnesium is a mineral that is involved in many enzymatic reactions in vivo. In addition, magnesium is abundant in bone in a living body, and its deficiency causes osteoporosis and osteomalacia. In addition, magnesium is involved in the biodistribution of calcium, the same divalent ion, and its deficiency causes ectopic calcifications such as kidney stones. In addition, magnesium deficiency is considered to contribute to diseases such as diabetes and hypertension.

【0003】これらの疾患に対するマグネシウムの投与
は治療的効果があるとの報告がある。また、疫学的な調
査からマグネシウムのカルシウムに対する相対的な摂取
不足は、虚血性心疾患の一因であると考えられている。
さらに、健康人においてもスポーツなどによるトレーニ
ング時の運動機能の向上にマグネシウムの摂取が有効で
あることも報告されている。
It has been reported that the administration of magnesium for these diseases has a therapeutic effect. In addition, epidemiological studies suggest that the relative lack of magnesium relative to calcium contributes to ischemic heart disease.
In addition, it has been reported that the intake of magnesium is effective for improving the motor function during training by sports or the like even in healthy people.

【0004】このように、多くの最近の研究からマグネ
シウムが生体内で重要な生理的役割を担っていることが
明らかにされてきている。現在、我が国においては、ヒ
トにおけるマグネシウムの1日当たりの目標摂取量は3
00mgとされているが、食生活のなかでこの目標を達
成するのは困難であり、実際の食事調査でもその摂取量
は200mg程度と推定され、100mg程度の摂取不
足が指摘され問題となっている。また、マグネシウムの
吸収は、食物繊維やカルシウム,燐などの他の食事成分
の影響を受けやすく、単に摂取量を増加させても生体に
有効に吸収され利用されない場合がある。
Thus, many recent studies have revealed that magnesium plays an important physiological role in vivo. At present, the target daily intake of magnesium in humans is 3 in Japan.
However, it is difficult to achieve this goal in the diet, and the actual dietary survey estimated that the intake was about 200 mg, and the lack of about 100 mg was pointed out and became a problem. I have. Further, the absorption of magnesium is easily affected by other dietary components such as dietary fiber, calcium, and phosphorus, and even if the intake amount is simply increased, it may be effectively absorbed by the living body and not used.

【0005】本発明の目的は、このような食生活の現状
に基づく栄養上の問題点を解決すべく、吸収性に優れた
マグネシウムの補給材とその利用技術を提供することに
ある。乳糖に、カルシウムの吸収促進作用があること
が、古くから知られており、牛乳のカルシウムの吸収が
良いことの一因と考えられている。また、乳糖は蔗糖と
比較すれば消化されにくく、乳糖不耐症は、その代表的
な例である。
It is an object of the present invention to provide a magnesium supplement excellent in absorbability and a technique for utilizing the same in order to solve such nutritional problems based on the current state of diet. It has been known for a long time that lactose has a calcium absorption promoting effect, and is considered to be one of the causes of the good calcium absorption of milk. Lactose is less digestible than sucrose, and lactose intolerance is a typical example.

【0006】本発明者らは、このような作用が乳糖に特
異的なものではなく、生体から分泌される消化酵素で消
化されにくい難消化性の糖質および糖アルコール全般に
共通した作用であるとの仮説を立て鋭意研究を重ねた。
その結果、難消化性の少糖であるフラクトオリゴ糖に乳
糖よりもむしろ強いミネラルの吸収促進作用があること
が解った。さらに、フラクトオリゴ糖のミネラル吸収促
進作用は、カルシウムに対するよりマグネシウムに対す
る方がより強力であることを発見した。この作用は、
クトオリゴ糖が大腸に到達した後、腸内細菌により発
酵を受け、その際に生じた有機酸によるものであると推
定される。
The present inventors have found that such an action is not specific to lactose, but an action common to all indigestible carbohydrates and sugar alcohols which are hardly digested by digestive enzymes secreted from the living body. I made a hypothesis that I repeated my research.
As a result, it was found that fructooligosaccharides, which are indigestible oligosaccharides, have a stronger mineral absorption promoting effect than lactose. In addition, the inventors have found that the effect of fructooligosaccharides on promoting mineral absorption is stronger for magnesium than for calcium. This effect is off
After La Kutoorigo sugar reaches the large intestine, undergo fermentation by intestinal bacteria, it is estimated to be due to an organic acid generated at that time.

【0007】[0007]

【課題を解決するための手段】すなわち本発明は、マグ
ネシウム源と、フラクトオリゴ糖を含有し、マグネシウ
ム源中のマグネシウムに対するフラクトオリゴ糖の配合
比率(重量比)が10〜400倍であることを特徴とす
るマグネシウム補給材並びに該マグネシウム補給材を含
有することを特徴とするマグネシウム欠乏症状の改善又
は予防剤を提供するものである。
That is, the present invention comprises a magnesium source, a fructooligosaccharide, and a magnesium salt.
Of fructooligosaccharides to magnesium in the source
Ratio containing magnesium supplementation material and the magnesium supplementation material, characterized in that (weight ratio) is 10 to 400 times
Amelioration of magnesium deficiency symptoms characterized by having
Provides a prophylactic agent .

【0008】本発明に用いられるマグネシウム源は特に
限定されるものではないが、食品添加物としては炭酸マ
グネシウム,塩化マグネシウム,硫酸マグネシウムが使
用できる。また、天然のマグネシウム源としてはマグネ
シウム含有量の高いアオノリ,昆布,ひじきなどの海草
類や、カカオ豆,ごま,大豆,アーモンド,ピーナッツ
などの種子類あるいは米糠,苦汁などの他、これらを加
工した食品が適している。
Although the magnesium source used in the present invention is not particularly limited, magnesium carbonate, magnesium chloride and magnesium sulfate can be used as food additives. Natural magnesium sources include seaweeds such as aonori, kelp, and hijiki, which contain high magnesium, seeds such as cacao beans, sesame, soybeans, almonds, peanuts, rice bran, bitter, and other processed foods. Is suitable.

【0009】ここで、マグネシウム源中のマグネシウム
とフラクトオリゴ糖の配合比率は、重量比でフラクトオ
リゴ糖がマグネシウムの10倍以上、通常は10〜40
0倍とすることが望ましい
Here, magnesium in a magnesium source
The ratio of fructooligosaccharide to fructo-oligosaccharide is
Rigo sugar is 10 times or more of magnesium, usually 10 to 40
It is desirable to make it 0 times .

【0010】マグネシウム欠乏症状の改善又は予防剤と
して用いることができる本発明のマグネシウム補給材
は、顆粒剤,カプセル剤,錠剤,粉剤,液剤などのあら
ゆる形態で摂取することができるが、食品に配合されて
摂取されてもよいことは言うまでもない。
An agent for ameliorating or preventing a magnesium deficiency symptom;
The magnesium supplement of the present invention, which can be used as a tablet, can be taken in any form such as granules, capsules, tablets, powders, and liquids, but it goes without saying that it may be taken in a food. No.

【0011】[0011]

【実施例】以下、実施例を挙げて具体的に説明するが、
これらは本発明を限定するものではない。実施例1 4週齢のSprague-Dawley系雄ラット(体重100〜11
0g)を標準固形試料(MF:オリエンタル酵母製)で
一週間飼育した後、1群7匹ずつとして試験に供した。
表1に示したように、マグネシウムを含まない飼料を対
照とし、これにマグネシウムのみを添加した飼料および
マグネシウムと難消化性オリゴ糖であるフラクトオリゴ
糖の比率が異なる6種類のマグネシウム補給材を添加し
た飼料をラットに14日間摂取させ、10日目から14
日目の4日間、マグネシウムの出納試験を行った。ま
た、マグネシウムの欠乏症状である耳介部および後頭部
の発赤症状についても観察した。飲料水には蒸溜水を用
い、飼料および飲料水は自由摂取とした。
The present invention will be specifically described below with reference to examples.
They do not limit the invention. Example 1 4-week-old male Sprague-Dawley rats (body weight 100-11)
0 g) was bred for one week with a standard solid sample (MF: manufactured by Oriental Yeast), and then subjected to the test in groups of 7 animals each.
As shown in Table 1, a feed containing no magnesium was used as a control, and a feed containing only magnesium and six kinds of magnesium supplements having different ratios of magnesium and fructooligosaccharide, which is an indigestible oligosaccharide, were added thereto. Rats were fed food for 14 days, and 14 days later,
On the 4th day, a balance test of magnesium was conducted. In addition, redness symptoms of the auricle and occipital region, which are symptoms of magnesium deficiency, were also observed. Distilled water was used as drinking water, and feed and drinking water were freely available.

【0012】[0012]

【表1】表1 試験試料組成表(%) Table 1 Table 1 Test sample composition table (%)

【0013】作製した飼料および回収した糞尿の一部を
磁性ルツボに秤量し、550℃の電気炉内で18時間灰
化後、0.1Nの塩酸に溶解しマグネシウム含有量をイオ
ンプラズマ発光分析装置(島津製作所製ICP−S50
00)を用いて測定し、含有率を求めた。飼料中のマグ
ネシウム含有率の実測値および糞尿中へのミネラル排泄
量から下式によりマグネシウムの吸収率および保留率を
算出した。
The prepared feed and a part of the collected manure are weighed in a magnetic crucible, ashed in an electric furnace at 550 ° C. for 18 hours, dissolved in 0.1N hydrochloric acid, and the magnesium content is measured by an ion plasma emission spectrometer. (ICP-S50 manufactured by Shimadzu Corporation
00) to determine the content. From the measured values of the magnesium content in the feed and the amount of mineral excreted in manure, the absorption rate and retention rate of magnesium were calculated by the following formulas.

【0014】[0014]

【数1】 (Equation 1)

【0015】結果は、表2に示す如く、本発明のマグネ
シウム補給材を摂取した群では、対照群およびマグネシ
ウムのみを摂取した群に比して耳介部および後頭部の発
赤症状の発症数および程度の軽減が認められ、マグネシ
ウムに対するフラクトオリゴ糖の重量が200倍以上の
G群およびH群では全く発症しなかった。また、表3に
示す如く、マグネシウム吸収率,保留率についてもマグ
ネシウムのみを摂取した群に比して、本発明のマグネシ
ウム補給材(マグネシウムに対するフラクトオリゴ糖の
重量が10倍以上)を摂取した群で有意(危険率5%以
下)に高値を示し、本発明のマグネシウム補給材が吸収
性および生体利用性に優れており、マグネシウム欠乏に
基づく発赤症状の改善効果も高いことが確認された。
As shown in Table 2, the number and extent of onset and degree of redness of the auricle and occiput were greater in the group receiving the magnesium supplement of the present invention than in the control group and the group receiving only magnesium. Was not observed in the G and H groups in which the weight of fructooligosaccharides with respect to magnesium was 200 times or more. Further, as shown in Table 3, the magnesium absorption rate and the retention rate of the group supplemented with the magnesium supplement of the present invention (the weight of fructooligosaccharides with respect to magnesium was 10 times or more) as compared with the group supplemented with magnesium alone. The magnesium supplement of the present invention was significantly high (hazard rate of 5% or less), indicating that the magnesium supplement of the present invention was excellent in absorbability and bioavailability, and also highly effective in improving redness symptoms due to magnesium deficiency.

【0016】[0016]

【表2】表2 本発明のマグネシウム補給材の皮膚発赤
症状の発症状況に及ぼす影響 −:発赤なし ±:殆ど発赤なし +:軽度発赤あり ++:中程度発赤あり +++:重度発赤あり (* :危険率5%以下で有意差あり)
Table 2 Effect of magnesium supplement of the present invention on the onset of skin redness -: No redness ±: Almost no redness +: Slight redness ++: Medium redness +++: Severe redness ( * : Significant difference at risk rate of 5% or less)

【0017】[0017]

【表3】表3 本発明のマグネシウム補給材のマグネシ
ウム吸収率および保留率に及ぼす影響 平均値±標準偏差 (n=7) (* :危険率5%以下で有意差あり)
Table 3 Effect of magnesium supplement of the present invention on magnesium absorption rate and retention rate Mean ± standard deviation (n = 7) ( * : significant difference is less than 5% risk level)

【0018】実施例2 4週齢のSprague-Dawley系雄ラット(体重100〜11
0g)を標準固形試料(MF:オリエンタル酵母製)で
一週間飼育した後、1群6匹ずつとし、試験に供した。
表4に示したように、マグネシウムを含まない飼料にマ
グネシウムのみを添加した飼料を対照とし、本発明の4
種類のマグネシウム補給材を添加した飼料をラットに1
4日間摂取させた。なお、飲料水には蒸溜水を用い、飼
料および飲料水は自由摂取とした。試験終了時にエーテ
ル麻酔下で開腹し、下大静脈より全血採血で屠殺し左右
の腎臓を摘出した。摘出した腎臓は重量を測定した後、
磁性ルツボに秤量し、550℃の電気炉内で18時間灰
化後、0.1Nの塩酸に溶解し、カルシウムをイオンプラ
ズマ発光分析装置(島津製作所製ICP−S5000)
を用いて測定し含有量を求めた。
Example 2 Male 4-year-old Sprague-Dawley rats (body weight 100-11)
0 g) was bred for one week with a standard solid sample (MF: manufactured by Oriental Yeast), and each group was composed of 6 animals, and subjected to the test.
As shown in Table 4, a feed containing only magnesium and a feed not containing magnesium was used as a control, and
Rats receive a diet supplemented with various magnesium supplements
They were ingested for 4 days. Distilled water was used as drinking water, and feed and drinking water were freely taken. At the end of the test, the abdomen was opened under ether anesthesia, sacrificed by whole blood sampling from the inferior vena cava, and the right and left kidneys were removed. After measuring the weight of the removed kidney,
Weighed in a magnetic crucible, ashed in an electric furnace at 550 ° C. for 18 hours, dissolved in 0.1N hydrochloric acid, and calcium ion-plasma emission spectrometer (ICP-S5000 manufactured by Shimadzu Corporation)
Was used to determine the content.

【0019】[0019]

【表4】表4 試験試料組成表(%) Table 4 Test sample composition table (%)

【0020】結果は、表5に示す如く、単にマグネシウ
ムのみを摂取した対照群に比して本発明のマグネシウム
補給材を摂取した群では腎臓中カルシウム量が低く、腎
結石の発症が抑えられ、腎臓重量も有意に軽く腎臓の肥
大もなかった。このことにより、本発明のマグネシウム
補給材はマグネシウム欠乏に基づく腎結石の発症を予防
する効果があることが確認された。
As shown in Table 5, the group receiving the magnesium supplement of the present invention had lower renal calcium content and suppressed the onset of renal calculi, as compared with the control group receiving only magnesium alone, as shown in Table 5. Kidney weight was also significantly lighter and there was no kidney enlargement. This confirms that the magnesium supplement of the present invention has an effect of preventing the onset of kidney stones due to magnesium deficiency.

【0021】[0021]

【表5】表5 本発明のマグネシウム補給材の腎臓に及
ぼす影響 平均値±標準偏差 (n=6) (* :危険率5%以下で有意差あり)
Table 5 Effect of magnesium supplement of the present invention on kidney Mean ± standard deviation (n = 6) ( * : Significant difference at 5% risk level or less)

【0022】実施例3 4週齢のSprague-Dawley系雄ラット(体重100〜11
0g)を標準固形試料(MF:オリエンタル酵母製)で
一週間飼育した後、1群7匹ずつとし、試験に供した。
表6に示したように、マグネシウムを含まない飼料にマ
グネシウムのみを添加した飼料およびこれに乳糖を添加
した飼料を対照とし、本発明のマグネシウム補給材を添
加した飼料をラットに14日間摂取させ、10日目から
14日目の4日間、マグネシウムの出納試験を行った。
飲料水には蒸溜水を用い、飼料および飲料水は自由摂取
とした。作製した飼料、回収した糞の分析およびマグネ
シウムの吸収率の算出は、実施例1と同様な方法で行っ
た。
Example 3 Four-week-old Sprague-Dawley male rats (body weight 100-11)
0 g) was bred for one week in a standard solid sample (MF: manufactured by Oriental Yeast), and then each group consisted of 7 animals, which were subjected to the test.
As shown in Table 6, a diet containing no magnesium and a diet containing only magnesium and a diet supplemented with lactose were used as controls, and rats were fed a diet supplemented with the magnesium supplement of the present invention for 14 days. Four days from the 10th day to the 14th day, a balance test of magnesium was conducted.
Distilled water was used as drinking water, and feed and drinking water were freely available. Analysis of the prepared feed, collected feces, and calculation of the magnesium absorption rate were performed in the same manner as in Example 1.

【0023】[0023]

【表6】表6 試験試料組成表(%) Table 6 Test sample composition table (%)

【0024】結果は、表7に示す如く、本発明のマグネ
シウム補給材を摂取した群のマグネシウム吸収率は、単
にマグネシウムのみを添加した飼料を摂取した対照群お
よびこれに乳糖を添加した飼料を摂取した対照群の両群
に比して有意(危険率5%以下)に高値を示し、本発明
のマグネシウム補給材が吸収性に優れていることが確認
された。
The results show that, as shown in Table 7, the magnesium absorption rate of the group receiving the magnesium supplement of the present invention was the same as that of the control group receiving only the diet supplemented with magnesium alone and the control group receiving the diet supplemented with lactose. It showed a significantly high value (risk rate: 5% or less) as compared with both control groups, and it was confirmed that the magnesium supplement of the present invention had excellent absorbability.

【0025】[0025]

【表7】表7 本発明のマグネシウム補給材のマグネシ
ウム吸収率 平均値±標準偏差 (n=7) (* :危険率5%以下で有意差あり)
Table 7 Table 7 Magnesium absorption rate of magnesium supplement of the present invention Mean ± standard deviation (n = 7) ( * : significant difference is less than 5% risk level)

【0026】実施例4 4週齢のSprague-Dawley系雄ラット(体重100〜11
0g)を標準固形試料(MF:オリエンタル酵母製)で
一週間飼育した後、1群7匹ずつとし、試験に供した。
表8に示したように、マグネシウムを含まない飼料にマ
グネシウムのみを添加した飼料および、さらにこの飼料
の倍量のマグネシウムを添加した飼料を対照とし、本発
明の2種類のマグネシウム補給材を添加した飼料をラッ
トに28日間摂取させ、24日目から28日目の4日
間、マグネシウムの出納試験を行った。試験終了時に、
ラットを屠殺解剖し、大腿骨を摘出した。なお、飲料水
には蒸溜水を用い、飼料および飲料水は自由摂取とし
た。作製した飼料、回収した糞の分析およびマグネシウ
ムの吸収率の算出は、実施例1と同様な方法で行った。
また、大腿骨中のカルシウムの分析は、実施例2と同様
な方法で行った。
Example 4 Male 4-year-old Sprague-Dawley rats (body weight 100-11)
0 g) was bred for one week in a standard solid sample (MF: manufactured by Oriental Yeast), and then each group consisted of 7 animals, which were subjected to the test.
As shown in Table 8, two types of magnesium supplements according to the present invention were added to a diet containing no magnesium and a diet to which only magnesium was added and a diet to which twice the amount of magnesium was further added as a control. Rats were ingested with the diet for 28 days, and a magnesium balance test was performed for 4 days from day 24 to day 28. At the end of the exam,
The rats were sacrificed and dissected, and the femurs were excised. Distilled water was used as drinking water, and feed and drinking water were freely taken. Analysis of the prepared feed, collected feces, and calculation of the magnesium absorption rate were performed in the same manner as in Example 1.
The analysis of calcium in the femur was performed in the same manner as in Example 2.

【0027】[0027]

【表8】表8 試験試料組成表(%) [Table 8] Table 8 Test sample composition table (%)

【0028】結果は、表9に示す如く、本発明のマグネ
シウム補給材を摂取した群のマグネシウム吸収率は、単
にマグネシウムのみを添加した飼料を摂取した対照群に
比して有意(危険率5%以下)に高値を示し、本発明の
マグネシウム補給材が吸収性に優れていることが確認さ
れた。本発明のマグネシウム補給材を添加したD群では
吸収量についてはマグネシウムを倍量添加した飼料を摂
取した群よりも多く、単にマグネシウムの摂取量を増加
させただけでは解決できない吸収量の向上をも得られる
ことが確認された。
The results show that, as shown in Table 9, the magnesium absorption rate of the group ingesting the magnesium supplement of the present invention was significantly (risk rate 5%) as compared with the control group ingesting the diet containing only magnesium alone. The following shows high values, and it was confirmed that the magnesium supplement of the present invention had excellent absorbability. In the group D to which the magnesium supplement of the present invention was added, the amount of absorption was larger than that of the group ingesting the feed containing twice the amount of magnesium. It was confirmed that it could be obtained.

【0029】[0029]

【表9】表9 本発明のマグネシウム補給材のマグネシ
ウム吸収率および吸収量 平均値±標準偏差 (n=7) (* :危険率5%以下で有意差あり)
Table 9 Magnesium absorption rate and absorption amount of magnesium supplement of the present invention Mean ± standard deviation (n = 7) ( * : significant difference is less than 5% risk level)

【0030】また、表10に示す如く、骨中カルシウム
の含有量も有意に増加し、マグネシウムの欠乏に基づく
骨化の減少が防止された。
Further, as shown in Table 10, the content of calcium in bone was also significantly increased, and a decrease in ossification due to magnesium deficiency was prevented.

【0031】[0031]

【表10】表10 本発明のマグネシウム補給材の大腿
骨カルシウム 含有率におよぼす影響 平均値±標準偏差 (n=7) (* :危険率5%以下で有意に高値)
Table 10 Effect of magnesium supplement of the present invention on femoral calcium content Mean ± standard deviation (n = 7) ( * : significantly higher than 5% risk level)

【0032】[0032]

【発明の効果】マグネシウムの欠乏は、腎結石や糖尿
病,高血圧症,虚血性心疾患などの疾患の危険因子であ
り、マグネシウムの摂取は健康人においてもスポーツな
どによるトレーニング時の運動機能の向上に有効であ
る。ヒトにおけるマグネシウムの1日当たりの目標摂取
量は300mgとされているが、実際の食生活のなかで
この目標を達成するのは困難であり、現状では100m
g程度の摂取不足が指摘されている。また、マグネシウ
ムの吸収は、他の食事成分の影響を受けやすく、単に摂
取量を増加させても生体に有効に利用されない場合があ
る。マグネシウムの吸収性や生体利用性に優れている本
発明のマグネシウム補給材を摂取すれば、マグネシウム
の摂取不足に起因する多くの疾患の予防や治療をするこ
とができる。
EFFECT OF THE INVENTION Magnesium deficiency is a risk factor for diseases such as kidney stones, diabetes, hypertension, and ischemic heart disease. Magnesium intake can improve the motor function of healthy people during training by sports and the like. It is valid. Although the target daily intake of magnesium in humans is 300 mg, it is difficult to achieve this target in an actual diet, and at present, 100 m
Insufficient intake of about g has been pointed out. In addition, magnesium absorption is susceptible to other dietary components, and simply increasing the intake may not be effectively used by the living body. Ingestion of the magnesium supplement of the present invention, which is excellent in magnesium absorbability and bioavailability, can prevent and treat many diseases caused by insufficient magnesium intake.

フロントページの続き (51)Int.Cl.7 識別記号 FI A61P 13/12 A61P 13/12 19/10 19/10 29/00 29/00 (72)発明者 滝沢 登志雄 埼玉県坂戸市千代田5の3の1 明治製 菓株式会社 生物科学研究所内 (56)参考文献 特開 平2−212(JP,A) 特開 昭60−72817(JP,A) 米国特許5002780(US,A) Congr.Int.Techno l.Pharm.,5th,Vol. 1,(1989)p.476−481 日本栄養・食糧学会誌,第44巻,第4 号,(1991)第287−291頁 (58)調査した分野(Int.Cl.7,DB名) A61K 33/06 A23L 1/304 A23L 1/308 A61K 47/36 A61P 3/02 A61P 13/12 A61P 19/10 A61P 29/00 CA(STN) EMBASE(STN) MEDLINE(STN)Continued on the front page (51) Int.Cl. 7 Identification code FI A61P 13/12 A61P 13/12 19/10 19/10 29/00 29/00 (72) Inventor Toshio Takizawa 5-3 Chiyoda, Sakado-shi, Saitama (1) Meiji Seika Co., Ltd. Biological Science Laboratory (56) References JP-A-2-212 (JP, A) JP-A-60-72817 (JP, A) US Patent 5002780 (US, A) Congr. Int. Techno l. Pharm. , 5th, Vol. 1, (1989) p. 476-481 Journal of the Japanese Society of Nutrition and Food Science, Vol. 44, No. 4, (1991) pp. 287-291 (58) Fields investigated (Int. Cl. 7 , DB name) A61K 33/06 A23L 1/304 A23L 1/308 A61K 47/36 A61P 3/02 A61P 13/12 A61P 19/10 A61P 29/00 CA (STN) EMBASE (STN) MEDLINE (STN)

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 マグネシウム源と、フラクトオリゴ糖を
含有し、マグネシウム源中のマグネシウムに対するフラ
クトオリゴ糖の配合比率(重量比)が10〜400倍で
あることを特徴とするマグネシウム補給材。
1. A magnesium source and fructooligosaccharide
Containing magnesium and magnesium
When the blending ratio (weight ratio) of ctooligosaccharide is 10 to 400 times
A magnesium supplement characterized by the fact that there is .
【請求項2】 請求項1記載のマグネシウム補給材を含
有るすことを特徴とするマグネシウム欠乏症状の改善又
は予防剤
2. A magnesium supplement as claimed in claim 1.
Amelioration of magnesium deficiency symptoms characterized by having
Is a prophylactic agent .
【請求項3】 マグネシウム欠乏症状が、発赤である請
求項2記載の改善又は予防剤
3. The magnesium deficiency symptom is redness.
The improvement or prevention agent according to claim 2 .
【請求項4】 マグネシウム欠乏症状が、腎結石である
請求項2記載の改善又は予防剤
4. The magnesium deficiency symptom is kidney stones.
The improving or preventing agent according to claim 2 .
【請求項5】 マグネシウム欠乏症状が、骨化減少であ
る請求項2記載の改善又は予防剤
5. The magnesium deficiency symptom is decreased ossification.
3. The improving or preventing agent according to claim 2 .
JP05103994A 1993-02-25 1994-02-25 Magnesium supplements and their use Expired - Lifetime JP3188583B2 (en)

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GB9525290D0 (en) * 1995-12-11 1996-02-07 Whittle Brian A Nutritional compositions
CA2240980A1 (en) 1995-12-16 1997-07-03 Onesta Nutrition, Inc. Dietary fiber delivery system
AT408416B (en) * 1996-07-19 2001-11-26 Norbert Fuchs PHARMACEUTICAL OR DIETETIC COMPOSITIONS
JPH10108647A (en) * 1996-10-08 1998-04-28 Meiji Seika Kaisha Ltd Mineral supplying material for patient after excision of stomach
US6989166B2 (en) 2001-12-20 2006-01-24 N.V. Nutricia Soft drink replacer
US6884445B2 (en) 2001-12-20 2005-04-26 N.V. Nutricia Matrix-forming composition containing pectin
JP4553604B2 (en) * 2003-06-30 2010-09-29 明治製菓株式会社 Function enhancing composition for general food, health functional food or health supplement and method thereof
WO2005007171A1 (en) 2003-07-18 2005-01-27 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Accelerator for mineral absorption and use thereof
JP4588403B2 (en) * 2004-10-04 2010-12-01 森永乳業株式会社 Method for producing calcium / magnesium-containing composition
WO2010114445A1 (en) * 2009-04-03 2010-10-07 X-International Aps Plant fiber product and method for its manufacture
JP6001108B2 (en) * 2015-02-02 2016-10-05 エクス−インターナショナル・エピエス Plant fiber product and method for producing the same
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Title
Congr.Int.Technol.Pharm.,5th,Vol.1,(1989)p.476−481
日本栄養・食糧学会誌,第44巻,第4号,(1991)第287−291頁

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